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Study identifier: NCT07239505 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Randomized Controlled Trial Evaluating Whether Pre-operative Trinase Reduces Post-operative Pain in Patients With Symptomatic Irreversible Pulpitis Compared to Placebo, Using VAS Scores and Analgesic Intake Over 48 Hours.

Condition: Symptomatic Irreversible Pulpitis (SIP) · Postoperative Pain After Endodontic Treatment · Endodontic Disease  ·  Sponsor: Fayoum University

PhaseNA
Planned participants182
Who can joinMale, 18 Years to 50 Years
Healthy volunteersNo

About this study

This study aims to determine whether Trinase, an enzyme-based anti-inflammatory medication, can reduce pain after root canal treatment in patients with symptomatic irreversible pulpitis. A total of 182 male patients aged 18 to 50 years who present with moderate to severe tooth pain will be randomly assigned to receive either a Trinase tablet or a placebo 30 minutes before treatment. All root canal procedures will be performed in a single visit using standard endodontic techniques. Pain levels will be measured on a Visual Analogue Scale (VAS) before treatment and at 6, 12, 24, and 48 hours after treatment. Patients will also record the number of pain-relief tablets they take during the first 48 hours. The goal of the study is to see whether Trinase can lower post-operative pain and reduce the need for analgesic medication compared with placebo. This information may help improve pain management for patients undergoing root canal therapy.

This description comes directly from the study's public registry record.

Talk to the study team

Ahmed Maged Negm, Associate Professor  ·  00201006600995  ·  ahmed.maged@mgu.edu.eg

Always discuss trial participation with your own doctor first.

Locations (1)

Fayoum UniversityAl Fayyum, Faiyum Governorate, EgyptRecruiting

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Source record: clinicaltrials.gov/study/NCT07239505